ライフサイエンスコーパス: glycosyltransferase

1 a systemic supply of FKRP protein acting as glycosyltransferase.

2 ransferase domain and a predicted C-terminal glycosyltransferase.

3 by cellulose synthase, a processive family-2 glycosyltransferase.

4 rimer installed onto protein targets by an N-glycosyltransferase.

5 separately from related Golgi-resident GT32 glycosyltransferases.

6 nto LacNAc and then elaborated by a panel of glycosyltransferases.

7 diverse range of substrates required for the glycosyltransferases.

8 the nucleotide-sugar substrates required by glycosyltransferases.

9 hat CgT represents a new member of GT-A-type glycosyltransferases.

10 s then extended to up to 11 HMOs by 4 robust glycosyltransferases.

11 by virtue of the inherent specificity of the glycosyltransferases.

12 amine (UDP-GlcNAc), a substrate for cellular glycosyltransferases.

13 inds the sugar nucleotide UDP-glucose, as do glycosyltransferases.

14 d serine-rich repeat adhesins by a series of glycosyltransferases.

15 process regulated by the availability of key glycosyltransferases.

16 ntrasted with common properties of canonical glycosyltransferases.

17 to the cell membrane and is hence exposed to glycosyltransferases.

18 encode seed-specific uridine 5'-diphosphate-glycosyltransferases.

19 the substrate specificities glycosidases and glycosyltransferases.

20 Golgi apparatus by glycoside hydrolases and glycosyltransferases.

21 ites that serve as monosaccharide donors for glycosyltransferases.

22 daptable to high-throughput screens of other glycosyltransferases.

23 dentified a unique hybrid protein dGT1 (dual glycosyltransferase 1) that contains two distinct domain

24 We show that the glycosyltransferases 1 and 2 (GT1 and GT2) are responsib

25 genes involved in zinc finger CCCH protein, glycosyltransferase, 1-aminocyclopropane-1-carboxylate o

26 yzed by the integral membrane lipid-to-lipid glycosyltransferase 4-amino-4-deoxy-L-arabinose transfer

27 ns proximal to the substrate binding site of glycosyltransferase 8 domain containing 1 (GLT8D1) are a

28 H3 looks like a glycosyltransferase, a family of enzymes that transfer c

29 In addition, a glycosyltransferase able to catalyze O-linked glucosylat

30 ped FKRP might circulate as an extracellular glycosyltransferase, able to exert a "glycan remodelling

31 ure of a previously disordered region in the glycosyltransferase active site and discuss its implicat

32 action of a polymerase (WbdA) containing two glycosyltransferase active sites.

33 This study, thus, identifies two of the glycosyltransferase activities involved in the synthesis

34 oreover, so far unknown chitin hydrolase and glycosyltransferase activities were detected using GlcNA

35 d TarS with respective alpha- and beta-(1-4) glycosyltransferase activities.

36 NleB glycosyltransferase activity inhibited GAPDH-TRAF3 bindi

37 inactive point mutants indicated that OGT-1 glycosyltransferase activity is dispensable for GABA neu

38 Heparin binding and glycosyltransferase activity may be involved in the func

39 tein-protein interaction and crucial for the glycosyltransferase activity of CgT in vitro and in vivo

40 l number of enzyme activities comprising the glycosyltransferase activity of class A PBP1b and the D,

41 Inhibition was dependent on the glycosyltransferase activity of NleB.

42 The glycosyltransferase activity of PBP1A, which aids in the

43 eriophora excreted-secreted products contain glycosyltransferase activity, these results demonstrate

44 nantly produced protein Sv0189 possessed UDP-glycosyltransferase activity.

45 a noncanonical isoform that lacks catalytic glycosyltransferase activity.

46 Homologous glycosyltransferases alpha-(1-->3)-N-acetylgalactosaminy

47 nstrated that the enzyme is active as both a glycosyltransferase and an HCF-1 protease.

48 njugates that takes advantage of recombinant glycosyltransferases and a corresponding sugar nucleotid

49 ile lineages by mutagenesis of five putative glycosyltransferases and biosynthetic genes.

50 Combinatorial biosynthesis of glycosyltransferases and deoxysugar synthesis enzymes is

51 g mechanisms that concentrate Golgi-resident glycosyltransferases and glycosidases in distinct Golgi

52 nzymatic labeling (or SEEL) uses recombinant glycosyltransferases and nucleotide-sugar analogues to a

53 y as a general approach for the screening of glycosyltransferases and other group-transfer enzymes.

54 neer glycans using different permutations of glycosyltransferases and to investigate biosynthetic pat

55 he bifunctional class A PBPs, which are both glycosyltransferases and transpeptidases, and monofuncti

56 among saponin biosynthesis genes, especially glycosyltransferases, and may be the driving force of th

57 ulfurylases, carbohydrate-sulfotransferases, glycosyltransferases, and one family 16 glycoside hydrol

58 ughput screening assay (FP-tag) for beta-Kdo glycosyltransferases, and use it to identify a class of

59 ent signaling pathways regulated by O-GlcNAc glycosyltransferase are thus fundamental for T cell biol

60 g target for control of the pathogen, as the glycosyltransferases are absent from mammalian hosts.

61 n to examples where genetic mutations within glycosyltransferases are associated with neurodegenerati

62 Multiple glycosyltransferases are essential for the proper modifi

63 Two closely related glycosyltransferases are responsible for the final step

64 O-linked-beta-N-acetylglucosamine (O-GlcNAc) glycosyltransferase as compared with naive cells.

65 neer glycans using different permutations of glycosyltransferases as well as to investigate biosynthe

66 Homologous glycosyltransferases assemble a similar core trisacchari

67 pparatus by a series of glycan synthases and glycosyltransferases before export to the wall.

68 s that nucleotide sugar donors for GT-A fold glycosyltransferases bind in similar positions and confo

69 in the center of the plant secondary product glycosyltransferase box (A389V) reduced the enzymatic ac

70 ditional ectopic expression of an engineered glycosyltransferase, "bump-and-hole" (BH)-GalNAc-T2, boo

71 c peptides of proteins, which modifies Tn by glycosyltransferase C1GalT1 with isotopically labeled UD

72 e associated with a gene encoding a putative glycosyltransferase called MUCILAGE-RELATED70 (MUCI70).

73 n on cells, where the products of individual glycosyltransferases can be selectively characterized or

74 Glycosyltransferases carry out important cellular functi

75 aryotic protein N-glycosylation, a series of glycosyltransferases catalyse the biosynthesis of a doli

76 m uses a catch and release approach in which glycosyltransferase-catalysed reactions are performed in

77 differs, with the enzyme WbbY possessing two glycosyltransferase catalytic sites solely responsible f

78 A series of glycosyltransferases catalyze sequential glycosylation o

79 otide sugars throughout the cell for various glycosyltransferase-catalyzed glycosylation reactions.

80 The UDP-glycosyltransferases, CcUGT4 and CcUGT5, catalyze consec

81 ed alpha repeat of the PGANT9A and PGANT9B O-glycosyltransferases confers distinct preferences for a

82 ly required for induction of Fut7 and Gcnt1, glycosyltransferases critical for selectin ligand biosyn

83 lyses reveal specific gene expansions in the glycosyltransferase, cytochrome P450, shikimate hydroxyc

84 Here we show that microinjection of the glycosyltransferase domain Afp18(G) into zebrafish embry

85 A glycosyltransferase domain and a deamidase domain of thi

86 llographic model for inhibition of the PBP1b glycosyltransferase domain by the potent substrate analo

87 The peptidoglycan glycosyltransferase domain of PBP1b is also considered a

88 cated between the coiled-coil region and the glycosyltransferase domain of SS4.

89 proteolytic fragment containing the putative glycosyltransferase domain was tested in isolation for a

90 mer in which each blade contains a GT-B-type glycosyltransferase domain with a typical Rossmann fold.

91 The csaA gene product contains a predicted glycosyltransferase domain with structural homology to G

92 a helices in addition to a typical GT-A-type glycosyltransferase domain.

93 we propose the linkage specificities of the glycosyltransferase domains are conserved in KpsC homolo

94 KpsC contains two retaining beta-Kdo glycosyltransferase domains belonging to family GT99 tha

95 he activated form of monosaccharides used by glycosyltransferases during glycosylation.

96 rases (ppGalNAc-Ts) on catalytic activity of glycosyltransferases during O-GalNAc glycan biosynthesis

97 we consider potential mechanisms connecting glycosyltransferase dysfunction to neurodegeneration.

98 tpM is the first member of a novel family of glycosyltransferase effectors employed to subvert hosts.

99 ations support the hypothesis that GT-A fold glycosyltransferases employ coevolving donor, acceptor,

100 n vivo glycoengineering technologies and the glycosyltransferase-enabled in vitro engineering method,

101 g penultimate sugar assembled by a different glycosyltransferase enables testing of the conformationa

102 of Xoc flagellin was altered by deletion of glycosyltransferase-encoding rbfC, but this had little e

103 or is regulated in part by the repertoire of glycosyltransferase enzymes (which make the glycan ligan

104 beta-Kdo counterparts were not identified as glycosyltransferase enzymes by bioinformatics tools and

105 The precise glycosyltransferase enzymes that mediate selectin-ligand

106 Namely, we highlight ArnT, a glycosyltransferase, EptA, a phosphoethanolamine transfe

107 tead of the canonical DxD motif of GT-A type glycosyltransferases, essential for enzyme activity and

108 Interestingly, KS biosynthesis specific glycosyltransferases expression was differentially regul

109 f the STELLO proteins indicate that they are glycosyltransferases facing the Golgi lumen.

110 epresented among the 98 currently recognized glycosyltransferase families in the Carbohydrate-Active

111 ential evolution of gene families, including glycosyltransferase family 25, whose activities are excl

112 gene, At3g57630, in clade E of the inverting Glycosyltransferase family GT47 as a candidate for the t

113 e of the adaptation by trypanosomes of beta3-glycosyltransferase family members to catalyze beta1-2 g

114 hat TbGT15, another member of the same beta3-glycosyltransferase family, encodes an equally divergent

115 B3GNT2 is in the largest mammalian glycosyltransferase family, GT31, but little is known ab

116 cularly redundant yet disease-relevant human glycosyltransferase family, the polypeptide N-acetylgala

117 AftD has a conserved GT-C glycosyltransferase fold and three carbohydrate-binding

118 Distinct features of a novel glycosyltransferase fold from a domain of unknown functi

119 IBP was first catalyzed by P450, and then by glycosyltransferase, followed by further storage or meta

120 ype O-glycan, and Tn-antigen; identified the glycosyltransferases for assembling novel nuclear O-Fuc-

121 ngs to a large family of membrane-associated glycosyltransferases for which the understanding of the

122 how that due to the asymmetric effect of the glycosyltransferase Fringe, different outcomes are gener

123 found that Toxoplasma utilizes a cytoplasmic glycosyltransferase from an ancient clade of CAZy family

124 tidine monophosphate-Kdo-dependent alpha-Kdo glycosyltransferase from LPS assembly is well characteri

125 lass B PBPs work together with transmembrane glycosyltransferases (FtsW and RodA) from the shape, elo

126 structural information exists that shows how glycosyltransferases functionally assemble with each oth

127 -undecaprenol (GlcNAc-P-Und) produced by the glycosyltransferase GacI.

128 Our results also suggested that a GT-C glycosyltransferase, GacL, transfers GlcNAc from GlcNAc-

129 crystallographic experiments showed that the glycosyltransferase Gat1 is specific for Skp1 in Toxopla

130 ene, a lipB (kpsS)-like gene, and a putative glycosyltransferase gene designated csaA (capsule synthe

131 s induce upregulated expression of the Gcnt1 glycosyltransferase gene in T cells mediating graft-vers

132 Furthermore, inactivation of each glycosyltransferase gene resulted in differentially impa

133 The glycosyltransferase gene, mannosyl (alpha-1,3-)-glycopro

134 Candidate uridine-diphosphate glycosyltransferase genes (UGTs) were selected based on

135 I (TbGnTI) among a set of putative T. brucei glycosyltransferase genes belonging to the beta3-glycosy

136 ion of a genomic island strongly enriched in glycosyltransferase genes involved in exopolysaccharide

137 d glycan array is self-renewable and reports glycosyltransferase genes required (or blocking) for int

138 Analysis of the expression of key glycosyltransferase genes revealed that p38alpha signali

139 f ATPase, cation transporter, kinase and UDP-glycosyltransferases genes.

140 an biosynthesis in mycobacteria involves two glycosyltransferases, GlfT1 and GlfT2, which have been t

141 ormation of this polymer is catalyzed by the glycosyltransferase GlfT2, a processive carbohydrate pol

142 tribution of processing machineries, such as glycosyltransferases, glycosidases, and nucleotide sugar

143 bject to multiple sequential and competitive glycosyltransferases/glycosidases.

144 discovered that the gene Mgat3 encoding the glycosyltransferase GnT-III is elevated in epithelial ov

145 ified by five sugars via the action of three glycosyltransferases, Gnt1, PgtA, and AgtA, which are re

146 The movement of a putative glycosyltransferase, GntB, requires the Sar1 and ARF1 GT

147 Bioinformatics analyses identified two glycosyltransferase (GT) domains in CslB.

148 rstood, largely because of the resistance of glycosyltransferase (GT) enzymes to structural character

149 WbbB contains three glycosyltransferase (GT) modules.

150 of LtpM uncovered a remote similarity to the glycosyltransferase (GT) toxin PaTox from the bacterium

151 nts) suggested that the a064r gene encodes a glycosyltransferase (GT) with three domains, each with a

152 e EpsHIJK proteins suggest EpsH and EpsJ are glycosyltransferases (GT) with a GT-A fold; EpsI is a GT

153 ylases, they constitute a distinct family of glycosyltransferases (GT108) that have likely been acqui

154 SuS belongs to family 4 of the glycosyltransferases (GT4) and contains an E-X7-E motif

155 is sufficient to stimulate its biosynthetic glycosyltransferase (GTase) activity.

156 lyzed the mechanism by which the cytosolic O-glycosyltransferase GtfA/B of Streptococcus gordonii mod

157 O-antigen can be modified by the activity of glycosyltransferase (gtr) operons acquired by horizontal

158 Three glycosyltransferases (GTs) are involved (WbdN, WbdO and

159 zymes such as glycoside hydrolases (GHs) and glycosyltransferases (GTs) are of growing importance as

160 Glycosyltransferases (GTs) are prevalent across the tree

161 HM is elongated by glycosyltransferases (GTs) from the cellulose synthase-l

162 al MUCILAGE-RELATED (MUCI) genes that encode glycosyltransferases (GTs) involved in the production of

163 c analysis identified six main proteins: two glycosyltransferases (GTs) TaGT43-4 and TaGT47-13; two p

164 identified the roles of three virus-encoded glycosyltransferases (GTs) that have four distinct GT ac

165 core subset of 152 genes encoding cell wall glycosyltransferases (GTs).

166 acterization of plant cell wall biosynthetic glycosyltransferases (GTs).

167 Like glycosyltransferases, H3 binds UDP-glucose, as shown by

168 Here, we examine a putative ecdysteroid glycosyltransferase, Hba_07292 (Hb-ugt-1), which was pre

169 is predicted to possess a typical GT-A-type glycosyltransferase, however, the activity remains unkno

170 l wall synthesis is achieved by a balance of glycosyltransferase, hydrolase and transglycosylase acti

171 previously unrecognized role for a specific glycosyltransferase in driving a CSC state.

172 ced intermediates that can be diversified by glycosyltransferases in a branch-selective manner to giv

173 Predictions for the function of two UDP-glycosyltransferases in flavonoid metabolism were confir

174 Consistently, new evidences reported glycosyltransferases in the blood, freely circulating or

175 sugars, which serve as donor substrates for glycosyltransferases in the lumen of Golgi vesicles and

176 A number of studies have implicated glycosyltransferases in the pathogenesis of neurodegener

177 nor and acceptor recognition among GT-B fold glycosyltransferases in the synthesis of diverse glycan

178 The substitution of glycosyltransferases in Toxoplasma and Pythium by an unr

179 rcially available and recombinantly produced glycosyltransferases including key N-acetylglucosaminylt

180 creased abundance of transcripts for several glycosyltransferases indicated the enzymes that may be i

181 udy, we show that using moenomycin and other glycosyltransferase inhibitors as templates, we were abl

182 mechanistic insights into the regulation of glycosyltransferase interactions, the transitions betwee

183 pid II, that is polymerized by peptidoglycan glycosyltransferases into glycan strands that are subseq

184 ations affecting exostosin-like 3 (EXTL3), a glycosyltransferase involved in heparan sulfate (HS) bio

185 nt with the predicted functions of the WbkD (glycosyltransferase involved in the biosynthesis of the

186 Fukutin-related protein (FKRP) is a glycosyltransferase involved in the functional glycosyla

187 R XYLEM9-LIKE [IRX9L]) encodes a family GT43 glycosyltransferase involved in xylan backbone biosynthe

188 inyltransferases (B3GNTs) are Golgi-resident glycosyltransferases involved in the biosynthesis of pol

189 fold of ppGalNAc-Ts in enzymatic activity of glycosyltransferases involved in the O-glycan biosynthes

190 role in the process; thus understanding the glycosyltransferases involved is key to identifying new

191 role in the process, thus understanding the glycosyltransferases involved is key to identifying new

192 irst evidence that isolated dysfunction of a glycosyltransferase is sufficient to cause a neurodegene

193 These data indicate that the glycosyltransferase is surprisingly promiscuous in its s

194 However, measuring the activity of glycosyltransferases is considerably more challenging.

195 urodegeneration and genetic variation within glycosyltransferases is not new.

196 ining member of a new class of cytoplasmic O-glycosyltransferases, is required and sufficient for fla

197 Herein, we developed an innovative glycosyltransferase labeling assisted mass spectrometry

198 and dependent on the expression of both like-glycosyltransferase (LARGE) and partially functional FKR

199 HepII) are controlled by phase-variable LOS glycosyltransferase (lgt) genes; we sought to define how

200 We show that this process requires the glycosyltransferase lh3 and that post-injury expression

201 this binding requires Mg(2+) Mutation of the glycosyltransferase-like metal ion binding motif in H3 g

202 synthesis, while UPEX1 encodes a family GT31 glycosyltransferase likely involved in galactosylation o

203 dentified colonization genes, epaX encodes a glycosyltransferase located in a variable region of the

204 Thus, bryophytes and algae likely lack the glycosyltransferase machinery required to synthesize api

205 y studies have suggested the significance of glycosyltransferase-mediated macromolecule glycosylation

206 issue of Cell, Liu et al. present FucoID, a glycosyltransferase-mediated tagging platform, to bioche

207 ontaining multiple cellulose synthase (CESA) glycosyltransferases mediates cellulose microfibril form

208 removal, or forced expression of Dll4 or the glycosyltransferase Mfng, blocks coronary plexus remodel

209 putative dehydrogenase MftD and the putative glycosyltransferase MftF.

210 These results explain how the glycosyltransferase modifies a progressively changing su

211 Several glycosyltransferases modify WTA to generate anomeric het

212 We study the functional role of glycosyltransferases modifying type B flagellin in the 0

213 Substitution of the predicted DXD glycosyltransferase motif with alanine residues abolishe

214 reactive antigen that was lost in a putative glycosyltransferase mutant, suggesting that this antigen

215 Moreover, we provide evidence that three glycosyltransferases (MXAN_3027/ExoK, MXAN_3262/ExoO and

216 ion by the Actinobacillus pleuropneumoniae N-glycosyltransferase (NGT) at every possible position alo

217 One such effector is the arginine glycosyltransferase NleB1 (NleB(CR) in C. rodentium) tha

218 -ALG3, ALG9, ALG12, ALG6, ALG8 and ALG10-are glycosyltransferases of the C-superfamily (GT-Cs), which

219 O-GlcNAc and leptin, whereas inhibition of O-glycosyltransferase (OGT) decreased O-GlcNAc and leptin.

220 Phloretin-2'-O-glycosyltransferase (P2'GT) catalyzes the last glycosyla

221 T-IV, and GnT-V in cells revealed that these glycosyltransferases, particularly GnT-IV, play importan

222 previously shown that loss of a conserved O-glycosyltransferase (PGANT4) in Drosophila results in ab

223 ers to the pathway in which Protein N- and O-glycosyltransferases (PGTases) sequentially add monosacc

224 that perform these reactions, polyisoprenyl-glycosyltransferases (PI-GTs) include dolichol phosphate

225 Bacterial glycosyltransferases play important roles in bacterial f

226 t, mice double heterozygous for Jag1 and the glycosyltransferase, Poglut1 (Rumi), start showing a sig

227 rase (Und-P GT), a flippase, and a polytopic glycosyltransferase (PolM GT) dedicated to attaching sug

228 ate-dependent dioxygenases and UDP-dependent glycosyltransferases potentially involved in diterpenoid

229 Such a dual glycosyltransferase-protease activity, which occurs in t

230 Thus, from a dual glycosyltransferase-protease, essentially single-activit

231 The H3 crystal structure shows that it has a glycosyltransferase protein fold.

232 Reconstitution of the glycosyltransferase reactions in extracts with radioacti

233 Mammalian glycosyltransferases recognize only the terminal LacNAc

234 onstraints, not stage-specific expression of glycosyltransferases, regulate GPI processing.

235 h the physiological function of blood stream glycosyltransferases remains unclear, they are likely re

236 Glycosyltransferases represent a large family of enzymes

237 transferase 1 gene (Pofut1), which encodes a glycosyltransferase required for NotchR-mediated cell-ce

238 The beta-Kdo glycosyltransferases responsible for synthesis of this c

239 ighlight the discovery of the monofunctional glycosyltransferases RodA and FtsW and describe how thes

240 gy to measure the group-transfer activity of glycosyltransferases sensitively using simple fluorescen

241 The glycosyltransferase ST6Gal-I is known to block homeostat

242 The glycosyltransferase ST6Gal-I, which adds alpha2-6-linked

243 This Synopsis considers recent advances in glycosyltransferase structural biology and site-directed

244 Structural comparison with other glycosyltransferases such as mouse Fringe reveals a nove

245 osyltransferase genes belonging to the beta3-glycosyltransferase superfamily.

246 tivity is normally inhibited by the O-linked glycosyltransferase Sxc (Super sex combs).

247 Among these is the glycosyltransferase TarM, a component of the WTA de novo

248 ugar and its linkage, here we identified the glycosyltransferase that completes the glycan and found

249 thin a GBS-specific gene encoding a putative glycosyltransferase that confers resistance to HMOs, sug

250 FKRP gene encodes for a glycosyltransferase that in vivo transfers a ribitol pho

251 mannosyltransferase A (PimA) is an essential glycosyltransferase that initiates the biosynthetic path

252 demonstrated that lymphostatin is a putative glycosyltransferase that is important in intestinal colo

253 GALGT2 (also B4GALNT2) encodes a glycosyltransferase that is normally confined to the neu

254 OGT is the only glycosyltransferase that modifies cytoplasmic and nuclea

255 NleB is a glycosyltransferase that modifies host proteins with N-a

256 l, deeply conserved family of plant-specific glycosyltransferases that add arabinose sugars to divers

257 mediators in vivo by engineering solubilized glycosyltransferases that attach galactose or sialic aci

258 (EmbB) belongs to a family of membrane-bound glycosyltransferases that build the lipidated polysaccha

259 by mixing-and-matching cell-free synthesized glycosyltransferases that can elaborate a glucose primer

260 s the Salmonella enterica SseK effectors are glycosyltransferases that modify host protein substrates

261 esized by membrane-integrated and processive glycosyltransferases that polymerize UDP-activated gluco

262 Quantitative PCR gene expression studies of glycosyltransferases that regulate display of sLe(X) rev

263 nserved glycolipid belong to a new family of glycosyltransferases that shares little homology with ot

264 ellulose synthase-like (CSL) families encode glycosyltransferases that synthesize the beta-1,4-linked

265 e a highly conserved family of transmembrane glycosyltransferases that work in concert with class B p

266 (also referred to as Gpi3) of the fungal UDP-glycosyltransferase, the first step in GPI biosynthesis,

267 This step is vital because glycosyltransferases, the enzymes mediating the glycosyl

268 omains that are diversely decorated by Golgi glycosyltransferases to become extended rodlike structur

269 that at each arm can be uniquely extended by glycosyltransferases to give access to highly complex as

270 rate biosynthetic pathway and use engineered glycosyltransferases to incorporate chemically tagged su

271 on (CDG) due to the exquisite sensitivity of glycosyltransferases to Mn concentration.

272 In the early 1980s, while using purified glycosyltransferases to probe glycan structures on surfa

273 the precursor, which is extended by cellular glycosyltransferases to produce 4-N(3)-Bn-alpha-O-glycan

274 ic strategy, using a limited number of human glycosyltransferases, to access a collection of 60 asymm

275 Moreover, whereas all glycosyltransferase toxins and effectors identified so f

276 N-terminal DUF1792 is a novel GT-D-type glycosyltransferase, transferring Glc residues to Glc-Gl

277 s study, we determine that CgT is a distinct glycosyltransferase, transferring GlcNAc residues to Glc

278 cluding a phage protein and a phase-variable glycosyltransferase ubiquitous among the diverse set of

279 espite the importance of uridine diphosphate glycosyltransferase (UGT) enzymes in drug and chemical m

280 iptomic data, identifying four UDP-dependent glycosyltransferase (UGT) genes as wound-induced and 12-

281 UDP-glycosyltransferase (UGT) plays a major role in the dive

282 Enzymes of the human UDP-glycosyltransferase (UGT) superfamily typically catalyze

283 dae, for example, are known to produce a UDP-glycosyltransferase (UGT) that negatively regulates ecdy

284 ed to involve a family 1 UDP-sugar dependent glycosyltransferase (UGT) to facilitate acetophenone acc

285 ncatula In addition, two uridine diphosphate glycosyltransferases, UGT73F18 and UGT73F19, which gluco

286 lated metabolites generated by UDP-dependent glycosyltransferases (UGTs) play critical roles in plant

287 Two montbretia UDP-dependent glycosyltransferases (UGTs), CcUGT1 and CcUGT2, catalyze

288 It is mediated by uridine-diphosphate glycosyltransferases (UGTs), that achieve their activity

289 ecaprenyl-phosphate (Und-P) sugar-activating glycosyltransferase (Und-P GT), a flippase, and a polyto

290 into the lumen of the Golgi apparatus where glycosyltransferases use them for the modification of pr

291 sm for modulating substrate preferences of O-glycosyltransferases via alternative splicing within spe

292 uding cytochrome P450 monooxygenases and UDP-glycosyltransferases, was shared between both treatments

293 erization and forming a complex with the O2a glycosyltransferase WbbM.

294 In contrast, O2c polymerization requires glycosyltransferases WbmV and WbmW, which interact with

295 As expected for a glycosyltransferase, we found that RDN1 and RDN2 protein

296 ring the substrate promiscuity of endogenous glycosyltransferases, we developed a single-step fluores

297 teen hypothetical proteins and uncategorized glycosyltransferases were also required for maximum comp

298 ntibiotic moenomycin that inhibits bacterial glycosyltransferases, which are essential for peptidogly

299 by a mechanism involving a membrane-embedded glycosyltransferase with a GT-C fold.

300 arge clostridial toxins, which are retaining glycosyltransferases with a DXD motif involved in bindin